Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5001493 | 6044771 | I | 5001493-1 | 20040406 | 20060504 | 20060512 | EXP | BR-MERCK-0605BRA00011 | MERCK HUMAN HEALTH DIVISION | 50 | YR | F | Y | 20060515 | LW | BRAZIL |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5001493 | 1007281962 | PS | VIOXX | 1 | ORAL | 021042 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5001493 | 1007281962 | PAIN |
Outcome of event
Event ID | OUTC COD |
---|---|
5001493 | DS |
5001493 | HO |
5001493 | LT |
Reactions reported
Event ID | PT |
---|---|
5001493 | CARDIAC DISORDER |
5001493 | INFECTION |
5001493 | PROTEUS INFECTION |
5001493 | TOXIC EPIDERMAL NECROLYSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5001493 | 1007281962 | 20040314 | 20040405 | 23 | DAY |